Rs12198986

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Orientationplus
Make rs12198986(A;A)
Make rs12198986(A;G)
Make rs12198986(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position7719826
is asnp
is mentioned by
dbSNPrs12198986
Exacrs12198986
PheGenIrs12198986
nextbiors12198986
hapmaprs12198986
1000 genomesrs12198986
hgdprs12198986
ensemblrs12198986
gopubmedrs12198986
geneviewrs12198986
scholarrs12198986
googlers12198986
pharmgkbrs12198986
gwascentralrs12198986
openSNPrs12198986
23andMers12198986
23andMe allrs12198986
SNP Nexus

SNPshotrs12198986
SNPdbers12198986
MSV3drs12198986
GMAF0.3283
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs12198986
PubMedID [PMID 18391951]
Condition Height
Gene BMP6
Risk Allele A
pValue 2.00E-011
OR 6.8
95% CI 4.84-8.76) % SD talle



[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.

[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs12198986
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary